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Supelco

Carpropamid

PESTANAL®, analytical standard

Sinónimos:

2,2-Dichloro-N-[1-(4-chlorophenyl)ethyl]-1-ethyl-3-methylcyclopropanecarboxamide

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About This Item

Fórmula empírica (notación de Hill):
C15H18Cl3NO
Número de CAS:
104030-54-8
Peso molecular:
334.67
Beilstein/REAXYS Number:
8395957
MDL number:
MFCD03095718
UNSPSC Code:
41116107
PubChem Substance ID:
329753885
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CCC1(C(C)C1(Cl)Cl)C(=O)NC(C)c2ccc(Cl)cc2

InChI

1S/C15H18Cl3NO/c1-4-14(10(3)15(14,17)18)13(20)19-9(2)11-5-7-12(16)8-6-11/h5-10H,4H2,1-3H3,(H,19,20)

Inchi Key

RXDMAYSSBPYBFW-UHFFFAOYSA-N

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General description

Carpropamid is widely used for the control of rice blast caused by Pyricularia oryzae. Carpropamid acts by inhibiting scytalone dehydratase enzyme involved in fungal melanin biosynthesis in a phytopathogenic fungus.

Application

Carpropamid may be used as a reference standard for the determination of the analyte in river water by liquid chromatography/time-of-flight mass spectrometry.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Environment
GHS09

hcodes

H411

pcodes

P273

Hazard Classifications

Aquatic Chronic 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCJ8255
BCBX4056
SZBD234XV
SZB8116XV
SZE8116X

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Tri Puji Priyatno et al.
TheScientificWorldJournal, 2012, 545784-545784 (2012-06-06)
The cyclic AMP- (cAMP-) dependent protein kinase A signaling pathway is one of the major signaling pathways responsible for regulation of the morphogenesis and pathogenesis of several pathogenic fungi. To evaluate the role of this pathway in the plant pathogenic
Carpropamid: a rice fungicide with two modes of action.
Thieron M, et al.
Pflanzenschutz-Nachrichten Bayer, 51(28), 257- 278 (1998)
A new on-line sample preparation system for the liquid chromatography/time-of-flight mass spectrometry simultaneous analysis of pesticides in river water.
Sasaki H, et al.
Analytical Sciences, 22(6), 835- 840 (2006)
Cryogenic X-ray crystal structure analysis for the complex of scytalone dehydratase of a rice blast fungus and its tight-binding inhibitor, carpropamid: the structural basis of tight-binding inhibition.
Nakasako M, et al.
Biochemistry, 37(28), 9931- 9939 (1998)
Young Seop Kwon et al.
Analytica chimica acta, 868, 60-66 (2015-03-31)
The sensitive detection of iprobenfos (IBF) and edifenphos (EDI) was successfully conducted by using a new aptamer-based colorimetric multi-aptasensor. The dissociation constants of this multi-target aptamer to both iprobenfos and edifenphos were found to be 1.67 μM and 38 nM
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